Label: HYPOCHLOROUS ACID HAND SANITIZER- hypochlorous acid liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated May 25, 2021

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  • Active ingredient

    Hypochlorous acid 100 mg/L. Purpose: Sanitation.

  • Purpose

    Kill germs and viruses, keep hands sanitated, protect health from disease or pandmics.

  • Use

    Hand disinfection for medical staff, or hand sanitation of families, enterprise or public places. It's suitable as well for hand sanitation of children, women and aged people.

  • Warnings

    For external use only.

    Do not use for eyes disinfection.

    Keep out of reach of children.

  • Do not use

    Do not use for eyes disinfection.

  • Cautions

    The product is normally not irritation to human skin or mucosa. If you feel uncomfortable in case of contact of eyes, please rinse or clean it with water. If swallowed and fee unwell, please get medical help.

  • Stop use

    If you feel uncomfortable in case of contact of eyes, please rinse or clean it with water. If swallowed and fee unwell, please get medical help.

  • Keep out of reach of children

    Keep out of reach of children.

  • Method to use

    Press the nozzle to soak the hand, keep rubbing hands for 1 minute.

  • Storage

    Keep away from heat and sunlight.

    Store in room temperature and in cool place.

  • Inactive ingredient

    Water

  • Package Label - Principal Display Panel

    HAHS500

  • INGREDIENTS AND APPEARANCE
    HYPOCHLOROUS ACID HAND SANITIZER 
    hypochlorous acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81934-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID50 mg  in 500 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81934-101-05500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/25/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/25/2021
    Labeler - Shenzhen Risai Medical Technology Co., Ltd (710909218)
    Registrant - A03 Lab of BTS (548009541)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Risai Medical Technology Co., Ltd710909218manufacture(81934-101) , label(81934-101)
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